Whole exome sequencing in dense families suggests genetic pleiotropy amongst Mendelian and complex neuropsychiatric syndromes

Whole Exome Sequencing (WES) studies provide important insights into the genetic architecture of serious mental illness (SMI). Genes that are central to the shared biology of SMIs may be identified by WES in families with multiple affected individuals with diverse SMI (F-SMI). We performed WES in 22...

Descripción completa

Detalles Bibliográficos
Autores principales: Ganesh, Suhas, Vemula, Alekhya, Bhattacharjee, Samsiddhi, Mathew, Kezia, Ithal, Dhruva, Navin, Karthick, Nadella, Ravi Kumar, Viswanath, Biju, Sullivan, Patrick F., Jain, Sanjeev, Purushottam, Meera
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9729597/
https://www.ncbi.nlm.nih.gov/pubmed/36476812
http://dx.doi.org/10.1038/s41598-022-25664-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9729597/
https://www.ncbi.nlm.nih.gov/pubmed/36476812
http://dx.doi.org/10.1038/s41598-022-25664-7

Ejemplares similares